FEMA Region VI PPE Request for Information.docx

Request for Information (RFI)

RFI70FBR620Q00000001

RFI FEMA REGION VI COVID-19 PPE

Federal Emergency Management Agency Department of Homeland Security FEMA Region VI Austin Texas Recovery Office on behalf of FEMA Region VI

REQUEST FOR INFORMATION – PERSONAL PROTECTIVE EQUIPMENT (PPE)

FACE MASKS, FACE SHIELDS, GOWN/OVERALLS, GLOVES

***This is potentially a FAR Part 18 Emergency Acquisitions or FAR 6.302-2 Unusual and compelling urgency requirement due to the novel Coronavirus (COVID-19) pandemic where a presidential Emergency Declaration was made, and potential Major Disaster Declarations may result. As such, the entirety of this Request for Information (RFI) is subject to change. Multiple authorities and/or singular authorities are subject to change and it is incumbent on all vendors to monitor this RFI continuously.

The U.S. Government / Federal Emergency Management Agency (FEMA) is seeking information and sources for immediate delivery of medical supplies and personal protective equipment (PPE). This is not an order for supplies.

The U.S. Government is interested in establishing multiple awards for immediate purchases of Face Masks, Gowns / Overalls, Gloves, and Face Shields / Eye Protection used in healthcare settings as described below. This will enable the United States to ensure sufficient availability of such items during national emergencies and/or pandemic events. The Government is concerned about the risks of disruption of any manufacturing facilities or supply chains located outside of the United States. Thus, offerors are advised to pay special attention to the instructions regarding manufacturing capability and/or supply chains located outside of the United States as well as the evaluation criteria related to manufacturing capability and foreign supply chains. The Government is concerned about the risks related to excessive pricing of critical PPE and intends only to acquire PPE at prices that it can determine are fair and reasonable. Thus, offerors are advised to pay special attention to the instructions regarding pricing.

Description/Tentative Items:

The Federal Emergency Management Agency (FEMA), Region VI is seeking information related to how interested contractors could provide the follow item(s) (Please note that this list is subject to change):

1. FACE MASKS

The following is a summary to provide clarification about the different types of acceptable Face Masks for facial protection that may be proposed as part of the requirement:

a. Surgical masks are fluid-resistant, disposable, and loose-fitting protection devices that create a physical barrier between the mouth and nose of the wearer and the immediate environment. FDA reviews and clears surgical masks under 21 CFR 878.4040 as Class II medical devices, which may be labeled as surgical, isolation, dental, or medical procedure masks. They may come with or without a face shield. These are often referred to as face masks, although not all face masks are regulated as surgical masks.

b. Face masks are disposable loose-fitting protection devices that create a physical barrier between the mouth and the nose of the wearer and the immediate environment. Face masks that are not cleared or approved by FDA preferably should demonstrate conformance to the following performance requirements through either a 1) Manufacturers declaration of conformity or through verification of testing by a 2) ISO 17025 accredited laboratory declaration of conformity to the following performance requirements:

c. Fluid resistance: Fluid resistance is met if the mask passes the test method below, or comparable test method, at any specific velocity as identified in the labeling. The mask shall be tested on a pass/fail basis at velocities specified in the standard.

ASTM F 1862: Standard Test Method for Resistance of Surgical Mask to Penetration by Synthetic Blood Viral or bacterial filtration performance (e.g., filters 95% of bacteria) Filtration testing (e.g., ASTM F2101–01 (Bacterial Filtration Efficiency) and ASTM F2299 (Particulate Filtration Efficiency)

d. Biocompatibility: Appropriate analysis and testing (such as that outlined in the ISO-10993-1 standard, “Biological Evaluation of Medical Devices Part 1: Evaluation and Testing within a Risk Management Process.”) must demonstrate the biocompatibility of the mask. Tests selected must be appropriate for expected duration and level of contact with the device (e.g., limited contact devices including skin). Masks should be tested on a pass/fail basis with respect to cytotoxicity, sensitization, and irritation.

2. GLOVES

Protection of healthcare workers and first responders from transmission of pathogens is essential to maintaining resilience of the U.S. healthcare system. Non-Sterile, Powder-Free, Patient Examination Gloves are one part of an infection control strategy and are examples of personal protective equipment (PPE) that is a disposable device intended for medical purposes that is worn on the examiner’s hand or finger to prevent contamination between patient and examiner. The appropriate use of PPE is an important component of the overall strategy of certain infection control guidelines.

The following is a list to provide clarification about the different types of acceptable Non-Sterile, Powder-Free, Patient Examination Gloves to protect against contamination that may be proposed as part of the requirement:

Patient Examination gloves are examples of personal protective equipment that are used to protect the wearer and/or the patient from the spread of infection or illness during medical procedures and examinations. Patient examination gloves are reviewed and cleared by the Federal and Drug Administration (FDA) as Class I reserved medical devices that requires a 510(k) premarket notification requiring registration and listing, under 21 CFR 880.6250.

Nitrile, Latex, Vinyl (PVC), or Polymer other than Vinyl patient examination gloves Length requirements for patient examination gloves must be a minimum of 220mm-230mm (8.6”- 9”) depending on glove size and material type Glove thickness for patient examination gloves must be a minimum of 8 mils Tensile strength as identified in relevant American Society for Testing and Materials (ASTM) standards Minimum unaged elongation percent as identified in relevant ASTM standards Acceptable Quality Level (AQL) for holes in MPa as identified in relevant ASTM standards

Scope of Work

The Contractor, as an independent organization and not as an agent of the Government, shall furnish all labor, materials, supplies, facilities, equipment, transportation and travel necessary to deliver one or more of the following acceptable Non-Sterile, Powder-Free, Patient Examination Gloves. Preference will be given in order by:

Nitrile, Non-Sterile, Powder-Free, Patient Examination Gloves Must meet ASTM D6319-19 standard specifications Must be registered and listed with FDA Must be snug or form fitting patient examination gloves Equivalent or similar to Dynarex #2513 Extra Small, Small, Medium, Large, Extra Large Latex, Non-Sterile, Powder-Free, Patient Examination Gloves Must meet ASTM D3578-19 standard specifications Must be registered and listed with FDA Must be snug or form fitting patient examination gloves Equivalent or similar to Medline #CUR8106 Extra Small, Small, Medium, Large, Extra Large Non-Latex, Non-Sterile, Powder-Free, Patient Examination Gloves (PVC/Polychloroprene) Must meet ASTM D5250-19 standard specifications (for Poly (vinyl chloride) or ASTM D6977 standard specifications (for polychloroprene) Must be registered and listed with FDA Must be snug or form fitting patient examination gloves Equivalent or similar to Innovative Healthcare #161300 or Smart Practice #433467 Extra Small, Small, Medium, Large, Extra Large A combination of the gloves described above may be acceptable to meet the Government’s requirement. Declaration of conformity to applicable standards listed above must be provided.

Product manufacturer and part number, description, and literature must be included in the proposal for consideration.

3. FACE SHIELDS / EYE PROTECTION

Protection of healthcare workers and first responders from transmission of pathogens is essential to maintaining resilience of the U.S. healthcare system. Eye protection is one part of an infection control strategy and is an example of personal protective equipment (PPE) that are devices used to help protect health care workers from splashes, sprays, and splatters of body fluids and infectious material in the air. Eye protection is designed to either cover the eyes only or to cover both the eyes and entire face. The appropriate use of PPE is an important component of the overall strategy of certain infection control guidelines.

Eye protection is an example of personal protective equipment that, depending on the type of device, can protect the eyes, face or associated mucous membranes from splashes, sprays, and airborne body fluids. Goggles provide direct eye protection for healthcare workers, whereas face shields offer a protective barrier to the entire facial area, eyes, nose and mouth. The choice of Eye protection is dependent on the level of risk of contamination.

Eye and face protection are manufactured in accordance with the American National Standards Institute (ANSI) International Safety Equipment Association (ISEA) Z.87.1-2010 standard. The following is a list of acceptable protective Eye protection based on their intended use and risk of contamination that may be proposed as part of the requirement:

Goggles – used to protect the eyes from splashes, sprays and infectious material Face shields – used to protect the facial area, including mucous membranes (eyes, nose, mouth) from splashes, sprays and infectious material

Scope of Work

The Contractor, as an independent organization and not as an agent of the Government, shall furnish all labor, materials, supplies, facilities, equipment, transportation and travel necessary to deliver one or more of the following acceptable Gowns. Preference will be given in order by:

Disposable Face shields Must meet ANSI/ISEA Z.87.1-2010 standard Must cover the front and sides of the face; be full face length with outer edges of the face shield reaching at least to the point of the ear, include chin and forehead protectors, and cover the forehead Include a single Velcro strap and or elastic strap Treated for anti-glare, anti-static, and anti-fogging properties Equivalent or similar to Medline NONFS300

Disposable Goggles (medical use) Must meet ANSI/ISEA Z.87.1-2010 standard Be indirectly vented Include solid side shields Include anti-fog lenses

Reusable Face Shields and Goggles (medical use) Must meet ANSI/ISEA Z.87.1-2010 standard Face shields should follow same criteria listed above for disposable face shield Goggles should follow same criteria listed above for disposable goggles

A combination of the eye protection described above may be acceptable to meet the Government’s requirement.

Declaration of conformity to applicable standards listed above must be provided.

Product manufacturer and part number, description, and literature must be included in the proposal for consideration.

Scope of Work

The Contractor, as an independent organization and not as an agent of the Government, shall furnish all labor, materials, supplies, facilities, equipment, transportation and travel necessary to deliver one or more of the following acceptable Face Masks. Preference will be given in order by:

Surgical masks cleared by FDA under 21 CFR 878.4040 as Class II medical devices; 510K number shall be provided by offeror if applicable.

Equivalent or similar to Medline NON27402 Face masks that are not cleared or approved by FDA but meet the above performance requirements through 1) manufacturer’s declaration of conformity or 2) ISO 17025 accredited laboratory declaration of conformity (please indicate which requirements are met and by which method 1) or 2) Equivalent or similar to Medline NON27122

A combination of the Face Masks described above may be acceptable to meet the Government’s requirement. Product manufacturer and part number, description, and literature must be included in the proposal for consideration.

4. GOWNS/COVERALLS

A. Gowns are examples of personal protective equipment that are intended to promote infection control practices and help protect patients and healthcare workers against microorganisms and body fluids during routine care, examinations, and medical procedures. The choice of gown is dependent on the level of risk of contamination. The American National Standards Institute/Association for the Advancement of Medical Instrumentation (ANSI/AAMI) PB70 establishes a system of classification for surgical and isolation gowns used in healthcare facilities, based on their liquid barrier performance. The ANSI/AAMI PB70 standard includes four standard tests to evaluate the barrier effectiveness of surgical gowns, isolation gowns, and surgical drapes. Based on the results of these standardized tests, four levels of barrier performance are defined, with Level 1 being the lowest level of protection, and Level 4 being the highest level of protection. ANSI/AAMI PB70 levels are as follows:

Level 1: Minimal risk, to be used, for example, during basic care, standard isolation, cover gown for visitors, or in a standard medical unit Level 2: Low risk, to be used, for example, during blood draw, suturing, in the Intensive Care Unit (ICU), or a pathology lab Level 3: Moderate risk, to be used, for example, during arterial blood draw, inserting an Intravenous (IV) line, in the Emergency Room, or for trauma cases Level 4: High risk, to be used, for example, during long, fluid intense procedures, surgery, when pathogen resistance is needed, or infectious diseases are suspected (non-airborne)

The following is a list of acceptable protective gowns based on their intended use and risk of contamination that may be proposed as part of the requirement:

i. Isolation gowns – disposable, typically non-sterile, used to protect health care personnel and patients from the transfer of microorganisms and body fluids in patient isolation situations, used for routine patient care in healthcare settings. Isolation gowns are not for use in surgical settings.

ii. Low risk of contamination – isolation gowns that claim minimal or low levels of barrier protection; ANSI/AAMI PB70 Level 1 or Level 2. These gowns should not be worn during surgical or invasive procedures, or for medium to high risk contamination patients care activities.

iii. Medium to high risk of contamination – isolation gowns that claim moderate to high barrier protection; ANSI/AAMI PB70 Level 3.

B) Surgical gowns – sterile, disposable gowns, devices that are intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from the transfer of microorganisms, body fluids, and particulate matter.

Surgical gowns are regulated by the Food and Drug Administration (FDA) under 21 CFR 878-4040 as a Class II medical device.

Low risk of contamination – surgical gowns that claim minimal or low levels of barrier protection; ANSI/AAMI PB70 Level 1 or Level 2.

Medium to high risk of contamination – surgical gowns that claim moderate to high barrier protection; ANSI/AAMI PB70 Level 3 and Level 4.

Scope of Work

The Contractor, as an independent organization and not as an agent of the Government, shall furnish all labor, materials, supplies, facilities, equipment, transportation and travel necessary to deliver one or more of the following acceptable Gowns.

All gowns May be woven or non-woven fabric.

Must be latex free Must be disposable Must meet ASTM F2407 standard Must meet CPSC standard 16 CFR Part 1610, Class 1 for flammability Must be clearly labeled with manufacturer, size, barrier protection level and dimensions/locations of critical and non-critical zones.

Preference will be given in order by:

Isolation Gowns Level 2 and Level 3 Barrier Protection Passes ANSI/AAMI PB70 Level 1 requirements or made of fabrics and seams that pass at a minimum AATCC 42 ≤ 4.5 g Passes ANSI/AAMI PB70 Level 2 requirements or made of fabric and seams that pass at a minimum AATCC 42 ≤ 1 g and AATCC 127 ≥ 20 cm H20 or EN 20811 ≥ 20 cm H20 Passes ANSI/AAMI PB70 Level 3 requirements or made of fabric and seams that pass at a minimum AATCC 42 ≤ 1 g and AATCC 127 ≥ 50 cm H20 or EN 20811 ≥ 50 cm H20 Passes ANSI/AAMI PB70 Level 4 requirements or made of fabric and seams that pass at a minimum ASTM F1671 or ISO 16604 ≥ 14 kPa Biocompatibility Materials used in the construction is non-sensitizing and non-irritating in accordance with ISO/ANSI/AAMI 10993-10 Natural Rubber Latex Gowns that contain natural includes the latex caution statement CFR 801.437, “THIS PRODUCT CONTAINS NATURAL RUBBER LATEX WHICH MAY CAUSE ALLERGIC REACTION.”

Design Full coverage, no open back Equivalent or similar to Medline NONLV200 and Medline NONLV315

Size Sizes: small, medium, regular/large, extra-large, extra-extra large

Surgical Gowns Barrier Protection Passes ANSI/AAMI PB70 Level 2 requirements or made of fabric and seams that pass at a minimum AATCC 42 ≤ 1 g and AATCC 127 ≥ 20 cm H20 or EN 20811 ≥ 20 cm H20 at the critical zones defined by ANSI/AAMI PB70 Passes ANSI/AAMI PB70 Level 3 requirements or made of fabric and seams that pass at a minimum AATCC 42 ≤ 1 g and AATCC 127 ≥ 50 cm H20 or EN 20811 ≥ 50 cm H20 at the critical zones defined by ANSI/AAMI PB70 Passes ANSI/AAMI PB70 Level 4 requirements or made of fabric and seams that pass at a minimum ASTM F1671 or ISO 16604 ≥ 14 kPa at the critical zones defined by ANSI/AAMI PB70 Passes EN 13795 standard performance gown requirements Passes EN 13795 high performance gown requirements Biocompatibility Materials used in the construction of surgical gowns passes ANSI/AAMI BE78 or ISO 10993-10 Sterility Assurance Level Sterile gown. Selected sterilization process for surgical gowns has a sterility assurance level of at least 10-6. Appropriate sterilization processes include those specified in ISO 11134 for moist heat, ISO 11135 for EtO, ISO 11137 for Gamma or ISO 13683 also for moist heat.

Flame Spread Materials used in the construction of surgical gowns meets the requirements for Class 1 “normal flammability” in accordance with 16 CFR Part 1610 before and after the conditioning specified in Section 9.

Natural Rubber Latex Gowns that contain natural rubber latex should be clearly labeled and include the latex caution statement CFR 801.437, “THIS PRODUCT CONTAINS NATURAL RUBBER LATEX WHICH MAY CAUSE ALLERGIC REACTION.”

Must be sterile Must be low lint Must meet Laser and ignition resistance standard (ISO 11810) Surgical Gowns (liquid penetration), (penetration by bloodborne pathogens) standard specifications Must be sterile Must be low lint Must meet Laser and ignition resistance standard (11810)3, and Level 4 small, medium, Design Full coverage, no open back Equivalent or similar to Medline DYNJP2002, Cardinal 9545, and Cardinal 9040

Size Sizes: small, medium, regular/large, extra-large, extra extra large (XXL)

Coveralls Single use Barrier Protection Made of fabrics and seams that pass at a minimum AATCC 42 ≤ 4.5 g Made of fabric and seams that pass at a minimum AATCC 42 ≤ 1 g and AATCC 127 ≥ 20 cm H20 or EN 20811 ≥ 20 cm H20 Made of fabric and seams that pass at a minimum AATCC 42 ≤ 1 g and AATCC 127 ≥ 50 cm H20 or EN 20811 ≥ 50 cm H20 Made of fabric and seams that pass at a minimum ASTM F1671 or ISO 16604 ≥ 14 kPa Pass NFPA 1999 coverall minimum performance requirements Pass EN14126 coverall minimum performance requirements (all types, all classes) Natural Rubber Latex Coveralls that contain natural includes the latex caution statement CFR 801.437, “THIS PRODUCT CONTAINS NATURAL RUBBER LATEX WHICH MAY CAUSE ALLERGIC REACTION.”

Size Sizes: medium, large, extra large

Offerors shall provide proof of meeting applicable standards as noted above, in their proposals.

Offerors shall demonstrate conformance to the applicable performance requirements as noted above by either 1) Manufacturers declaration of conformity or 2) ISO 17025 accredited laboratory declaration of conformity (please indicate which requirements are met and by which method).

Product manufacturer and part number, description, and literature must be included in the proposal for consideration.

Instructions: Please provide the following information to be considered as a source to provide the described items.

Company Name:

DUNS Number:

Contact Name, Phone and Email:

Initial Cost Schedule Requested:

Quantity Requested*

Face Masks

30,000

Gloves

30,000

Face Shields/Eye Protection

30,000

Gowns/Coveralls

30,000

* Quantity requested is subject to change.

Delivery Locations/Addresses:

Given the uncertainty of what/when/where of the supplies to be delivered, vendors are asked to provide their ability/inability to provide delivery to the following locations*:

Little Rock, AR; Fort Smith, AR; Fayetteville, AR; Springdale, AR; Jonesboro, AR; New Orleans, LA; Baton Rouge, LA; Shreveport, LA; Metairie, LA; Lafayette, LA; Albuquerque, NM; Las Cruces, NM; Rio Rancho, NM; Santa Fe, NM; Roswell, NM; Oklahoma City, Tulsa, OK; OK; Norman, OK; Broken Arrow, OK; Edmond, OK; Houston, TX; San Antonio, TX; Dallas, TX; Austin, TX; Fort Worth, TX; El Paso, TX; Arlington, TX; Corpus Christi, TX; Region VI Headquarters in Denton; TX; and Beeville, TX.

* Locations are subject to change and are not to be considered all-inclusive. Further, a combination of delivery locations may be determined to be sent to specific locations within cities, FEMA office locations, medical centers, and other municipalities/locales as deemed necessary.

Hours of Performance: The vendor shall be available to schedule all delivery activities with the appropriate delivery point of contact after award. Unless stated otherwise, delivery acceptance hours are Mon – Fri 8am-2pm for that particular time zone.

Shipping Information:

*All product cases shall be packed in the vendor’s standard commercial casing, which shall be shipped on industry standard size pallets (48L inches by 40W inches, 4-way). Pallets must arrive stretch-wrapped with no less than 10 layers of covering. Material shall be stacked so the total height of each pallet and material does not exceed 55 inches. Pallets shall be hardwood and designed for pickup from all four sides. Shoring and bracing shall be used to prevent shifting during transit. Contractor shall use edge protectors, angle boards or corner protectors on each pallet to prevent shifting and reduce damages during movement.

*Please note that orders may not require shipments in pallets, but this information is used as a measure of a minimum capability among vendors.

Responses:

Responses to this RFI shall be emailed to the Contracting Officer (Andrea.Tubbs@FEMA.DHS.gov), Contract Specialist Horacio Fernandez (Horacio.Fernandez@FEMA.DHS.gov), and Contract Specialist Sandra Shanks (Sandra.Shanks@FEMA.DHS.gov) on or before 10:00 AM, Central Standard Time (CST) on Monday May 2nd, 2020. We will be accepting any information over the next 30 days.

Here is an additional list of personnel to send a carbon copy to, as other contract specialists/officers may be utilizing this list for ordering of supplies*:

Johnny.Lyonsiii@ FEMA.DHS.gov; Charmayne.Collins@FEMA.DHS.gov; Charmaine.Hoffman@FEMA.DHS.gov; Neddra.Tucker@FEMA.DHS.gov; Doris.Prier@FEMA.DHS.gov; Sherrie.Stewart@FEMA.DHS.gov; Janet.Payne@FEMA.DHS.gov; and Gisselle.Arias@FEMA.DHS.gov.

*Personnel from this list may be removed as deemed necessary. Additional personnel may also be listed based on the needs of FEMA in its entirety.

All responses to the RFI must be submitted electronically. Each response must be single-spaced and typewritten in 12-point Times New Roman font and in the English language. Each response must be in .doc, .docx, or .pdf format with every page of the response separately numbered. Also, each response must be no more than ten (10) 8½” by 11” pages in total (excluding applicable diagrams and charts) and all pages must be combined as one attachment.

All responses shall provide the following administrative information:

Name, mailing address, phone number, and email of designated Point of Contact – See also above highlighted areas and table.

Business type (large business, small business, etc.) based upon the North American Industry Classification System (NAICS) code(s). Please refer to Federal Acquisition Regulation FAR 19 for additional information on Small Business Size Standards.

Questions:

Questions regarding this RFI shall be submitted in writing by email to the Contracting Officer (Andrea.Tubbs@FEMA.DHS.gov), Contract Specialist Horacio Fernandez (Horacio.Fernandez@FEMA.DHS.gov), and Contract Specialist Sandra Shanks (Sandra.Shanks@FEMA.DHS.gov) no later 10:00 AM, CST on Friday, April 10th, 2020. Verbal questions will NOT be accepted. Questions will be answered by posting answers to the website where the RFI has been posted; accordingly, questions shall NOT contain proprietary information. No questions received after 10:00 AM, CST on Friday, April 10th, 2020 will be answered.

Vendor Meetings:

Upon receipt of responses, the government may, or may not, schedule informal informational sessions with vendors. Meetings may be held via teleconference.

Summary:

THIS IS A REQUEST FOR INFORMATION (RFI) ONLY.

This is not a Request for Quote (RFQ) or a Request for Proposal (RFP). The information provided in the RFI is subject to change and is not binding to the government. FEMA has not made a commitment to procure any of the items discussed, and respondents are advised that the U.S. government will not pay for any information or administrative costs incurred in response to this RFI; all costs associated with responding to this RFI will be solely at the interested party’s expense.

All submissions become government property and will not be returned. This RFI does not constitute a solicitation for bids, proposals or quote and is not to be construed as a commitment by the government to issue an RFQ/RFP or award of a contract as a result of this request.

Furthermore, FEMA is not at this time seeking proposals and will not accept unsolicited proposals. Not responding to this RFI does not preclude participation in any future RFP, if any is issued. It is the responsibility of potential offerors to monitor the solicitation website(s) such as betaSAM or eBuy, where a potential solicitation of a future requirement may be published.

Any document submitted in response to this RFI that contains confidential information must be marked on the outside as containing confidential information. Each page upon which confidential information appears must be marked as containing confidential information. The confidential information must be clearly identifiable to the reader wherever it appears. All other information will not be treated as confidential.

All information marked confidential in RFI responses is only for the government’s planning use. Confidential information may be reviewed by contractors; subject to a non-disclosure agreement (NDA) including, but not limited to, commercial or financial data obtained by the respondent’s submitted documents. Otherwise, no information marked confidential included in this document or in conversations connected to it may be disclosed to any other party outside of the government.

Clauses:

FAR Subpart 52-215(3)--Request for Information or Solicitation for Planning Purposes (Oct 1997)

The government does not intend to award a contract on the basis of this solicitation or to otherwise pay for the information solicited except as an allowable cost under other contracts as provided in subsection FAR 31.205-18 bid and proposal costs (https://www.acquisition.gov/content/part-31-contract-cost-principles-and-procedures#i1085142) of the Federal Acquisition Regulation.

Although “proposal” and “offeror” are used in this Request for Information, your response will be treated as information only. It shall not be used as a proposal.

This solicitation is issued for the purpose of obtaining information from vendors on its ability to source and deliver products within 5 (five) days after receipt of an order.